2-Bromopropane → 4-Bromo-1-isopropyl-1H-pyrazole

HRID 64057

反応式

HRID 64057 の反応式
[Br:1][C:2]1[CH:3]=[N:4][NH:5][CH:6]=1.C([O-])([O-])=O.[K+].[K+].Br[CH:14]([CH3:16])[CH3:15]>CN(C=O)C>[Br:1][C:2]1[CH:3]=[N:4][N:5]([CH:14]([CH3:16])[CH3:15])[CH:6]=1

参加物

5

実験手順

To a solution of 4-bromo-1H-pyrazole (5 g, 34 mmol) in DMF (70 ml) were added K2CO3 (11.83 g, 85.6 mmol, 2.5 eq.) and 2-bromopropane (6.3 g, 51.36 mmol, 1.5 eq.) and the mixture was stirred at RT for 12 h. The mixture was quenched and extracted as in Intermediate Example 5(a). The solvent was distilled off and the crude residue was purified by column chromatography (60-120 silica gel, 20% ethyl acetate in hexane) to afford the product in 89% yield (5.8 g). 1H NMR (300 MHz, DMSO-d6): δ 8.01 (s, 1H), 7.50 (s, 1H), 4.49-4.43 (m, 1H), 1.38 (d, 6H).

後処理

  1. customThe mixture was quenched
  2. extractionextracted as in Intermediate Example 5(a)
  3. distillationThe solvent was distilled off
  4. customthe crude residue was purified by column chromatography (60-120 silica gel, 20% ethyl acetate in hexane)
  5. customto afford the product in 89% yield (5.8 g)

出典と根拠

ORDレコード
ord-27cb84df084c4cb9be2332bc6cd068a1
出典データセット
uspto-grants-2016_09
特許番号
US09447091B2

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